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Median Arcuate Ligament Syndromedrwalidagmy
61 years old man with epigastric pain and vomiting
The median arcuate ligament is a fibrous arch unites the diaphragmatic crura .
in some people, the ligament inserts low or celiac art originate high.
young patients (20–40 y), F : M  CT angiograms:            focal narrowing in the proximal celiac axis.             inspiration and expiration          2ry signs poststenotic dilatation and collaterals.ttt   : surgery.
 angulations and narrowing of the proximal celiac axis.  Sagittal 3D image of a patient with epigastric pain
Sagittal (MIP) of a patient with recurrent abdominal pain reveals focal calcified plaque.
Prostglandin induced hyperostosisdrwalidagmy
Caffey disease(ICH) AD  . subperiosteal bone formation before 6 months, M:f  1:1 General hyperirritability, fever and anorexia, painful, firm soft-tissue swelling. PGE TTT infants with cyanotic heart disease  cortical hyperostosis that mimics ICH.  PGE serum levels elevated  Indomethacin.
  DD   - Physiological in infant not more than 4 m.    - trauma.    - Hypervitaminosis A.    - scurvy    - prostaglandin E1 and E2 administration , 42% of infants for more than 30 days; this increases to 100% in more than 60 days.8    - infection (including syphilis)    - metastatic neuroblastoma.
Thank you

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Med arcuate lig syndrome1

  • 1. Median Arcuate Ligament Syndromedrwalidagmy
  • 2. 61 years old man with epigastric pain and vomiting
  • 3.
  • 4.
  • 5.
  • 6.
  • 7. The median arcuate ligament is a fibrous arch unites the diaphragmatic crura .
  • 8. in some people, the ligament inserts low or celiac art originate high.
  • 9. young patients (20–40 y), F : M  CT angiograms: focal narrowing in the proximal celiac axis. inspiration and expiration 2ry signs poststenotic dilatation and collaterals.ttt : surgery.
  • 10.  angulations and narrowing of the proximal celiac axis. Sagittal 3D image of a patient with epigastric pain
  • 11. Sagittal (MIP) of a patient with recurrent abdominal pain reveals focal calcified plaque.
  • 13.
  • 14.
  • 15.
  • 16.
  • 17.
  • 18. Caffey disease(ICH) AD  . subperiosteal bone formation before 6 months, M:f 1:1 General hyperirritability, fever and anorexia, painful, firm soft-tissue swelling. PGE TTT infants with cyanotic heart disease cortical hyperostosis that mimics ICH. PGE serum levels elevated Indomethacin.
  • 19.   DD - Physiological in infant not more than 4 m. - trauma. - Hypervitaminosis A. - scurvy - prostaglandin E1 and E2 administration , 42% of infants for more than 30 days; this increases to 100% in more than 60 days.8 - infection (including syphilis) - metastatic neuroblastoma.